IQVIA

Site Activation Manager (evergreen)

IQVIA(1 year ago)

HybridFull TimeSenior$167,008 - $222,182 (estimated)Regulatory Affairs
Apply Now

About this role

This role leads regulatory and site activation efforts for clinical studies and multi-protocol programs, supporting study initiation and maintenance across regions. It provides regulatory and scientific input for pre-award and business development activities and contributes regulatory intelligence to support program execution. The position partners with study management teams and clients to ensure compliant delivery of study authorizations and approvals.

View Original Listing

Required Skills

  • Site Activation
  • Regulatory Strategy
  • Project Management
  • Budget Management
  • Technical Writing
  • GCP
  • ICH
  • Leadership
  • Stakeholder Management
  • Quality Management

+4 more

Qualifications

  • Bachelor's Degree Life Sciences
IQVIA

About IQVIA

iqvia.com

IQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.

View more jobs at IQVIA

ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.

© All Rights Reserved. ApplyBlast.com